Three Phases of DiGeorge/22q11 Deletion Syndrome Pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes

SUMMARY: DiGeorge, or 22q11 Deletion Syndrome (22q11DS), the most common survivable human genetic deletion disorder, is caused by deletion of a minimum of 32 contiguous genes on human chromosome 22, and presumably results from diminished dosage of one, some, or all of these genes—particularly during...

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Hlavní autoři: Meechan, D.W., Maynard, T.M., Tucker, E.S., LaMantia, A-S.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2010
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3770287/
https://ncbi.nlm.nih.gov/pubmed/20833244
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ijdevneu.2010.08.005
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